Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

Παρόμοια τεκμήρια

• Mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: high prevalence and phenotypic variation
  ανά: Bernal, S, κ.ά.
  Έκδοση: (2003)
• Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa
  ανά: Riveiro-Alvarez, Rosa, κ.ά.
  Έκδοση: (2008)
• Mutation Spectrum of EYS in Spanish Patients with Autosomal Recessive Retinitis Pigmentosa
  ανά: Barragán, Isabel, κ.ά.
  Έκδοση: (2010)
• Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa
  ανά: Paloma, E, κ.ά.
  Έκδοση: (2002)
• Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa
  ανά: Yang, Yin, κ.ά.
  Έκδοση: (2016)